Echogenic mass with posterior
shadowing suggesting calcification.
Mass may extend into the
thoracic cavity making it impossible to distinguish from a calcified
thoracic neuroblastoma.
Mass is extrapleural and
affects one or more ribs.
Ribs near center of mass is
eroded or destroyed whereas the ribs near the periphery are deformed or
eroded.
CYSTIC HYGROMA OF THE CHEST WALL AND AXILLA (3-5)
Multiseptate fluid-filled
mass (resembles a cystic hygroma in other locations).
70-90% of postnatally
diagnosed cystic hygromas are found in the neck, and about 20% are located
in the axilla (2). Other locations have a prevalence of under 10% (3).
Prenatal diagnosis of axillary cystic hygroma have been previously
described (2-4).
Involves the chest wall in a
similar fashion to cystic hygroma, but there is marked involvement of the
subcutaneous tissue. This distinguishes lymphangiectasia from cystic
hygroma and subcutaneous edema from fetal hydrops.
HEMANGIOMA
Found in
Klippel-Trenaunay-Weber syndrome.
May have thick septations
and usually extend onto an extremity.
Other rare masses such as
melanoma would presumably be homogeneously solid.
REFERENCES
Brar MK, Cubberley DA, Baty
BJ et.al. Chest wall hamartoma in a fetus. J Ultrasound Med
1988;7:217-220.
Masuzaki H, Masuzaki M,
Ishimaru T et.al. Chest wall hamartoma diagnosed prenatally using
ultrasonography and computed tomography. J Clin Ultrasound 1996;24:83-85.
Reichler A, Bronshtein M.
Early prenatal diagnosis of axillary cystic hygroma. J Ultrasound Med
1995;14:581-584.
Anderson NG, Kennedy JC.
Prognosis in fetal cystic hygroma. Aust NZ J Obstet Gynecol 1992;32:36.
Hoffman-Tretin J, Koenisberg
M, Ziprowski M. Antenatal demonstration of axillary cystic hygroma. J
Ultrasound Med 1994;7:233.